Cite
HARVARD Citation
Willig, L. et al. (2015). Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings. Lancet. 3 (5), pp. 377-387. [Online].
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Willig, L. et al. (2015). Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings. Lancet. 3 (5), pp. 377-387. [Online].